The following data is part of a premarket notification filed by Argon Medical Corp. with the FDA for Needles Used In Angiographic Proced..
| Device ID | K772369 |
| 510k Number | K772369 |
| Device Name: | NEEDLES USED IN ANGIOGRAPHIC PROCED. |
| Classification | Trocar |
| Applicant | ARGON MEDICAL CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DRC |
| CFR Regulation Number | 870.1390 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1977-12-27 |
| Decision Date | 1978-01-24 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 10886333208507 | K772369 | 000 |
| 10886333208491 | K772369 | 000 |
| 10886333208484 | K772369 | 000 |
| 10886333208460 | K772369 | 000 |